Validation Specialist - Cork | Global Pharmaceutical Leader
Validation Specialist - Cork | Global Pharmaceutical Leader

Validation Specialist - Cork | Global Pharmaceutical Leader

Full-Time 36000 - 60000 Β£ / year (est.) No home office possible
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Deloitte

At a Glance

  • Tasks: Lead validation processes and ensure compliance in a dynamic pharmaceutical environment.
  • Company: Join Deloitte, a global leader in delivering impactful solutions across various sectors.
  • Benefits: Enjoy potential long-term contracts and the chance to work in a high-growth industry.
  • Why this job: Be part of a high-impact programme with a globally recognised company making a difference.
  • Qualifications: Experience in validation, strong documentation skills, and familiarity with regulatory frameworks required.
  • Other info: This role is based in Cork and offers opportunities for professional growth.

The predicted salary is between 36000 - 60000 Β£ per year.

At Deloitte, we make an impact that matters for our clients, our people, our profession, and in the wider society by delivering the solutions and insights they need to address their most complex business challenges.

Find out if this opportunity is a good fit by reading all of the information that follows below.

AMS is a global workforce solutions partner committed to creating inclusive, dynamic, and future-ready workplaces. We help organisations adapt, grow, and thrive in an ever-evolving world by building, shaping, and optimising diverse talent strategies.

We partner with Deloitte Ireland to support their contingent recruitment processes. Acting as an extension of their recruitment teams, we connect them with skilled interim and temporary professionals, fostering workplaces where everyone can contribute and succeed.

On behalf of Deloitte, AMS are looking for a Validation Specialist for an initial 12-month contract based in Cork.

Purpose of the role:

This is a fantastic opportunity to join a high-impact programme with one of the most established and globally recognised pharmaceutical companies in the world. You will play a key role in ensuring software and systems are validated in line with strict regulatory standards. The initial contract is for 12 months, with good potential for extension, offering long-term contracting opportunities in a high-growth, life sciences environment.

What you\’ll do:

Lead and support validation and testing processes in line with SDLC methodologies

Create and execute validation plans, protocols, and reports

Ensure regulatory compliance through comprehensive documentation and risk management

Analyse data and manage documentation using tools such as Veeva Vault, Oracle, SQL Server, and Jira

Collaborate with cross-functional teams to deliver compliant and high-quality solutions

Maintain and update validation documentation and reports to meet ongoing compliance requirements

The skills you\’ll need:

Proven experience in validation and software testing processes

Strong documentation skills, including authoring validation plans and protocols

Familiarity with regulatory frameworks and compliance in the Life Sciences sector

Hands-on experience with tools such as Veeva Vault, Oracle, SQL Server, and Jira

Solid understanding of the Software Development Lifecycle (SDLC)

Next steps

This client will only accept workers operating via an Umbrella or PAYE engagement model.

If you are interested in applying for this position and meet the criteria outlined above, please click the link to apply and we will contact you with an update in due course.

AMS, a Recruitment Process Outsourcing Company, may in the delivery of some of its services be deemed to operate as an Employment Agency or an Employment Business

Validation Specialist - Cork | Global Pharmaceutical Leader employer: Deloitte

Deloitte is an exceptional employer, offering a dynamic and inclusive work culture that prioritises employee growth and development. As a Validation Specialist in Cork, you will be part of a high-impact programme within a globally recognised pharmaceutical leader, benefiting from long-term contracting opportunities and the chance to work with cutting-edge technologies in a thriving life sciences environment.
Deloitte

Contact Detail:

Deloitte Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Validation Specialist - Cork | Global Pharmaceutical Leader

✨Tip Number 1

Familiarise yourself with the specific regulatory frameworks relevant to the pharmaceutical industry. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to compliance and quality assurance.

✨Tip Number 2

Gain hands-on experience with the tools mentioned in the job description, such as Veeva Vault and SQL Server. If you can showcase your proficiency with these tools during discussions, it will significantly boost your chances of standing out.

✨Tip Number 3

Network with professionals already working in validation roles within the pharmaceutical sector. Engaging with them can provide insights into the role and may even lead to referrals, which can be a great advantage in the hiring process.

✨Tip Number 4

Prepare to discuss your experience with the Software Development Lifecycle (SDLC) in detail. Being able to articulate your understanding and how you've applied it in past roles will show that you're well-equipped for the responsibilities of this position.

We think you need these skills to ace Validation Specialist - Cork | Global Pharmaceutical Leader

Validation and Software Testing Processes
Documentation Skills
Regulatory Compliance Knowledge
Risk Management
Data Analysis
Veeva Vault Proficiency
Oracle Database Experience
SQL Server Familiarity
Jira Usage
Software Development Lifecycle (SDLC) Understanding
Cross-Functional Collaboration
Attention to Detail
Analytical Skills
Problem-Solving Skills

Some tips for your application 🫑

Understand the Role: Read the job description thoroughly to understand the key responsibilities and required skills for the Validation Specialist position. Tailor your application to highlight how your experience aligns with these requirements.

Highlight Relevant Experience: Emphasise your proven experience in validation and software testing processes. Use specific examples from your past roles that demonstrate your familiarity with regulatory frameworks and compliance in the Life Sciences sector.

Showcase Documentation Skills: Since strong documentation skills are crucial for this role, include examples of validation plans, protocols, or reports you have authored. This will showcase your ability to maintain comprehensive documentation and ensure regulatory compliance.

Use Keywords from the Job Description: Incorporate keywords and phrases from the job description into your CV and cover letter. This not only shows that you have read the job posting carefully but also helps your application stand out in applicant tracking systems.

How to prepare for a job interview at Deloitte

✨Understand the Regulatory Landscape

Familiarise yourself with the regulatory frameworks relevant to the pharmaceutical industry. Being able to discuss how these regulations impact validation processes will demonstrate your expertise and commitment to compliance.

✨Showcase Your Documentation Skills

Prepare examples of your previous work involving validation plans and protocols. Highlighting your strong documentation skills will reassure the interviewers that you can maintain the high standards required in this role.

✨Be Ready to Discuss Tools

Brush up on your knowledge of tools like Veeva Vault, Oracle, SQL Server, and Jira. Be prepared to explain how you've used these tools in past projects, as practical experience with them is crucial for this position.

✨Demonstrate Team Collaboration

Since the role involves working with cross-functional teams, think of examples where you've successfully collaborated with others. Emphasising your ability to work well in a team will show that you're a good fit for their collaborative environment.

Validation Specialist - Cork | Global Pharmaceutical Leader
Deloitte
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